| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000317968 |
| Start |
94662425:94662425(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1589A>G |
| AA Mutation |
p.Tyr530Cys(p.Y530C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000317968 |
| Start |
94586439:94586439(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.915G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000317968 |
| Start |
94618133:94618133(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1050G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |